drugset / Trial / NCT02560753

Feasibility Study in Subjects With Mild to Moderate Alzheimer's Disease

NCT02560753 ↗

Phase 1/2 Completed 36 enrolled T3D Therapeutics, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The study is a randomized, parallel, 4-dose design in subjects with mild-to-moderate Alzheimer's Disease. Subjects will be randomized to one of 4 doses of T3D-959. Subjects will be evaluated for changes from baseline in cerebral metabolic rate of glucose (FDG-PET imaging), functional connectivity of the hippocampus (BOLD-fMRI), and cognitive function (ADAS-Cog11 and DSST) as well as assessed for safety and tolerability to T3D-959. An expanded access extension is planed to provide access to study medication to subjects who have completed the main study and requested continued use.

Timeline

Start
2015-07
Primary completion
2016-05-30
Completion
2016-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject DB959 Small molecule 3 mg Oral
Subject DB959 Small molecule 10 mg Oral
Subject DB959 Small molecule 15 mg Oral
Subject DB959 Small molecule 30 mg Oral
Subject DB959 Small molecule 90 mg Oral

Indications